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1.
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.
Am J Hum Genet
; 110(1): 120-145, 2023 01 05.
Article
in English
| MEDLINE | ID: mdl-36528028
2.
Divergent growth of the transient brain compartments in fetuses with nonsyndromic isolated clefts involving the primary and secondary palate.
Cereb Cortex
; 34(2)2024 01 31.
Article
in English
| MEDLINE | ID: mdl-38365268
3.
Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders.
Am J Hum Genet
; 108(8): 1450-1465, 2021 08 05.
Article
in English
| MEDLINE | ID: mdl-34186028
4.
Atypical fetal brain development in fetuses with non-syndromic isolated musculoskeletal birth defects (niMSBDs).
Cereb Cortex
; 33(21): 10793-10801, 2023 10 14.
Article
in English
| MEDLINE | ID: mdl-37697904
5.
Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects.
Am J Hum Genet
; 107(6): 1170-1177, 2020 12 03.
Article
in English
| MEDLINE | ID: mdl-33232677
6.
De novo variants in MPP5 cause global developmental delay and behavioral changes.
Hum Mol Genet
; 29(20): 3388-3401, 2020 12 18.
Article
in English
| MEDLINE | ID: mdl-33073849
7.
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.
Am J Hum Genet
; 110(3): 548, 2023 Mar 02.
Article
in English
| MEDLINE | ID: mdl-36868207
8.
Comparison of accelerated 3-D spiral chemical shift imaging and single-voxel spectroscopy at 3T in the pediatric age group.
Pediatr Radiol
; 45(9): 1417-22, 2015 Aug.
Article
in English
| MEDLINE | ID: mdl-25824958
9.
Clinical correlates in an experimental model of repetitive mild brain injury.
Ann Neurol
; 74(1): 65-75, 2013 Jul.
Article
in English
| MEDLINE | ID: mdl-23922306
10.
A novel syndrome caused by the E410K amino acid substitution in the neuronal ß-tubulin isotype 3.
Brain
; 136(Pt 2): 522-35, 2013 Feb.
Article
in English
| MEDLINE | ID: mdl-23378218
11.
Emerging cerebral connectivity in the human fetal brain: an MR tractography study.
Cereb Cortex
; 22(2): 455-64, 2012 Feb.
Article
in English
| MEDLINE | ID: mdl-21670100
12.
Effect of neonatal seizure burden and etiology on the long-term outcome: data from a randomized, controlled trial.
Ann Child Neurol Soc
; 1(1): 53-65, 2023 Mar.
Article
in English
| MEDLINE | ID: mdl-37636014
13.
Association of cerebral metabolic rate following therapeutic hypothermia with 18-month neurodevelopmental outcomes after neonatal hypoxic ischemic encephalopathy.
EBioMedicine
; 94: 104673, 2023 Aug.
Article
in English
| MEDLINE | ID: mdl-37392599
14.
Progressive multifocal cystlike cortical tubers in tuberous sclerosis complex: Clinical and neuropathologic findings.
Epilepsia
; 50(12): 2648-51, 2009 Dec.
Article
in English
| MEDLINE | ID: mdl-19624715
15.
Reusable Client-Side JavaScript Modules for Immersive Web-Based Real-Time Collaborative Neuroimage Visualization.
Front Neuroinform
; 11: 32, 2017.
Article
in English
| MEDLINE | ID: mdl-28507515
16.
Interictal High Frequency Oscillations Detected with Simultaneous Magnetoencephalography and Electroencephalography as Biomarker of Pediatric Epilepsy.
J Vis Exp
; (118)2016 12 06.
Article
in English
| MEDLINE | ID: mdl-28060325
17.
Sturge-Weber Syndrome: Brain Magnetic Resonance Imaging and Neuropathology Findings.
Pediatr Neurol
; 58: 25-30, 2016 05.
Article
in English
| MEDLINE | ID: mdl-26706049
18.
A FreeSurfer-compliant consistent manual segmentation of infant brains spanning the 0-2 year age range.
Front Hum Neurosci
; 9: 21, 2015.
Article
in English
| MEDLINE | ID: mdl-25741260
19.
MR connectomics: a conceptual framework for studying the developing brain.
Front Syst Neurosci
; 6: 43, 2012.
Article
in English
| MEDLINE | ID: mdl-22707934
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